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Chemical Structure| 223671-18-9 Chemical Structure| 223671-18-9

Structure of 223671-18-9

Chemical Structure| 223671-18-9

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Product Details of [ 223671-18-9 ]

CAS No. :223671-18-9
Formula : C9H6BrNO
M.W : 224.05
SMILES Code : BrC1=CC2=C[N+]([O-])=CC=C2C=C1
English Name :7-Bromoisoquinoline 2-oxide
MDL No. :MFCD09953462
InChI Key :QLRDQGRZLHHBPE-UHFFFAOYSA-N
Pubchem ID :22665927

Safety of [ 223671-18-9 ]

Application In Synthesis of [ 223671-18-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 223671-18-9 ]

[ 223671-18-9 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 223671-18-9 ]
  • [ 868-85-9 ]
  • [ 1632231-85-6 ]
YieldReaction ConditionsOperation in experiment
80% In toluene at 100℃; for 20h; Sealed tube; Green chemistry; regioselective reaction;
  • 2
  • [ 223671-18-9 ]
  • [ 407-25-0 ]
  • [ 75-50-3 ]
  • [ 1803206-17-8 ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran; dichloromethane at 0 - 20℃; regioselective reaction;
  • 3
  • [ 223671-18-9 ]
  • [ 1801986-20-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: tetrahydrofuran; dichloromethane / 0 - 20 °C 2: tetrabutyl ammonium fluoride / tetrahydrofuran; acetonitrile / 1 h / 60 °C
  • 4
  • [ 223671-18-9 ]
  • [ 58794-09-5 ]
YieldReaction ConditionsOperation in experiment
94% With hydrogenchloride; titanium(III) chloride In water; acetonitrile at 20℃; for 1h;
82% With diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate In dichloromethane at 31℃; for 16h; Sealed tube; Irradiation;
  • 5
  • [ CAS Unavailable ]
  • [ 223671-18-9 ]
  • [ 2064318-88-1 ]
YieldReaction ConditionsOperation in experiment
62% With iodine In dichloromethane at 120℃; for 5h; regioselective reaction;
  • 6
  • [ 104-53-0 ]
  • [ 223671-18-9 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine; (R)-2-(diphenyl(trimethylsilyloxy)methyl)pyrrolidine; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate In tetrahydrofuran at 0 - 20℃;
  • 7
  • [ 104-53-0 ]
  • [ 223671-18-9 ]
  • [ CAS Unavailable ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
80 % ee With (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate In tetrahydrofuran at 0 - 20℃; enantioselective reaction;
  • 8
  • [ 223671-18-9 ]
  • [ 2218516-80-2 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine; (R)-2-(diphenyl(trimethylsilyloxy)methyl)pyrrolidine; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate / tetrahydrofuran / 0 - 20 °C 2: tetrahydrofuran / 18 h / 20 °C
 

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